JP6502798B2 - Base material for wet friction material and method for manufacturing the same - Google Patents

Base material for wet friction material and method for manufacturing the same Download PDF

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JP6502798B2
JP6502798B2 JP2015174140A JP2015174140A JP6502798B2 JP 6502798 B2 JP6502798 B2 JP 6502798B2 JP 2015174140 A JP2015174140 A JP 2015174140A JP 2015174140 A JP2015174140 A JP 2015174140A JP 6502798 B2 JP6502798 B2 JP 6502798B2
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JP2017048887A (en
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真美 籏
真美 籏
義人 藤巻
義人 藤巻
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Aisin Chemical Co Ltd
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本発明は、湿式クラッチ及び湿式ブレーキ等に組み込むことができる湿式摩擦材用基材及びその製造方法に関する。   The present invention relates to a wet friction material substrate that can be incorporated into a wet clutch, a wet brake, and the like, and a method of manufacturing the same.

従来、湿式摩擦材を用いた湿式変速機や湿式制動機が、トルク伝達や制動等に利用されている。例えば、湿式変速機は、複数枚の湿式摩擦材と複数枚のセパレータプレートとが小さなクリアランスを介して交互に配置され、両者を圧接・離間することでトルク伝達・非伝達を行う構造となっている。そして、湿式変速機内には、この圧接・離間における湿式摩擦材の摩擦低減や摩擦に伴う摩擦熱を吸収する目的等で潤滑油が供給されている。
近年、低燃費化を目指してこの湿式変速機の小型化が進められており、上述の湿式摩擦材のサイズ縮小や構成枚数の低減が要求されている。即ち、より小さいサイズ、より少ない構成枚数の湿式摩擦材によって、従来と同等の摩擦性能を発揮させるという、湿式摩擦材の高性能化が求められている。
BACKGROUND Conventionally, a wet transmission or a wet brake using a wet friction material is used for torque transmission, braking, and the like. For example, a wet transmission has a structure in which a plurality of wet friction materials and a plurality of separator plates are alternately disposed via a small clearance, and torque transmission and non-transmission are performed by pressing and separating the two. There is. In the wet transmission, lubricating oil is supplied for the purpose of reducing the friction of the wet friction material in pressure contact and separation and absorbing the frictional heat associated with the friction.
In recent years, the miniaturization of this wet transmission has been promoted in order to reduce fuel consumption, and the above-mentioned reduction in size of the wet friction material and reduction in the number of components are required. That is, there is a demand for improving the performance of a wet friction material in which the same friction performance as in the past is exhibited by the wet friction material having a smaller size and a smaller number of components.

この湿式摩擦材の高性能化に際して、湿式摩擦材に利用される基材の高性能化が必要となる。湿式摩擦材用基材は、一般に、抄紙工法によって製造される。即ち、基材を形成する繊維及び摩擦特性を付与する摩擦調整材やその他所望の特性を付与する充填材等の必要な成分が配合された分散液から固形分を抄き取った抄紙が湿式摩擦材の基材となる。従って、基材内で摩擦調整材等の充填材は、均一且つランダムに配置されることとなる。ここで、摩擦特性は摩擦面での充填材の配置が大きく影響を及ぼしているため摩擦面に摩擦調整剤等の充填材を多く配置することで摩擦特性を改良することが可能となる。このような技術としては、下記特許文献1及び下記特許文献2が知られている。   In order to improve the performance of the wet friction material, it is necessary to improve the performance of the base material used for the wet friction material. The wet friction material base is generally manufactured by a paper making method. That is, paper made from solid matter from a dispersion containing the necessary components such as fibers forming the base material, friction modifiers imparting frictional properties, and other fillers imparting desired properties is wet rubbed. It becomes the base material of the material. Therefore, fillers such as friction modifiers are uniformly and randomly arranged in the base material. Here, since the arrangement of the filler on the friction surface largely affects the friction characteristic, it is possible to improve the friction characteristic by arranging a large amount of filler such as a friction modifier on the friction surface. As such a technique, the following patent document 1 and the following patent document 2 are known.

特開2012−097360号公報JP, 2012-097360, A 特開2011−252554号公報JP, 2011-252554, A

上記特許文献1には、微細な気泡を含有させた溶媒中に繊維材料と充填材(摩擦調整材)とを添加して攪拌すると、表面積の大きい繊維材料が溶媒上方に移動し、表面積の小さい充填材は溶媒下方へ移動する。この現象を利用し、一面側に充填剤を偏在させた湿式摩擦材を得る技術が開示されている。
また、上記特許文献2には、繊維材料と充填材(摩擦調整材)とが分散されたスラリー状抄紙原料から抄紙工法によって水分を吸水する際に、その水流を制御することによって、充填材を、得られる湿式摩擦基材の一面側に偏在させる技術が開示されている。
According to Patent Document 1 above, when a fiber material and a filler (friction modifier) are added to a solvent containing fine air bubbles and stirred, the fiber material having a large surface area moves to above the solvent, and the surface area is small. The filler moves down the solvent. A technique is disclosed that uses this phenomenon to obtain a wet friction material having a filler unevenly distributed on one side.
Further, in Patent Document 2, when water is absorbed from the slurry-like papermaking material in which the fiber material and the filler (friction modifier) are dispersed by the paper making method, the filler is controlled by controlling the water flow. There is disclosed a technique for unevenly distributing on one side of the obtained wet friction substrate.

しかしながら、上記のいずれも、抄造中に充填材(摩擦調整材)を偏在させる技術であるため、抄造された抄紙中の摩擦面側に摩擦調整材が多く配置されるように偏在させることや、最大限、抄紙中の摩擦面側のみに偏在させることもできるが、抄紙中の充填材を摩擦面側に偏在させると、摩擦面側の気孔が減少し、その結果、潤滑油の吸収が制限されることにより湿式摩擦材に要求される所望特性が得にくくなる。つまり、充填材の摩擦面における偏在量と気孔率のバランスをとるのが難しい場合があり、要求仕様によってはバランスをとる事ができない場合が起こり得る。   However, since any of the above is a technology for unevenly distributing the filler (friction modifier) during papermaking, it should be unevenly distributed so that a large amount of the friction modifier is disposed on the friction surface side in papermaking. Although it is possible to unevenly distribute only on the friction side during papermaking, when the filler in papermaking is unevenly distributed to the friction side, pores on the friction side decrease, as a result, absorption of lubricating oil is limited. As a result, it becomes difficult to obtain the desired characteristics required of the wet friction material. That is, it may be difficult to balance the uneven distribution amount and the porosity on the friction surface of the filler, and there may be cases where the balance can not be balanced depending on the required specifications.

本発明は、上記従来の技術に鑑みてなされたものであり、湿式摩擦材用基材中の気孔を充分に確保しながら、湿式摩擦材用基材に配合される充填材、特に摩擦調整材等の粒状物を摩擦面にのみ顕著に偏在させることができる湿式摩擦材用基材及びその製造方法を提供することを目的とする。   The present invention has been made in view of the above-mentioned prior art, and a filler, particularly a friction modifier, to be blended with a wet friction material substrate while sufficiently securing pores in the wet friction material substrate. And the like. It is an object of the present invention to provide a substrate for a wet friction material and a method of manufacturing the same, in which particulate matter such as can be significantly localized only on the friction surface.

本発明は以下の通りである。
請求項1に記載の湿式摩擦材用基材は、抄造によって形成された繊維層と、前記繊維層の一面に粒状物によって形成された気孔を有する粒状層と、を備え、
前記気孔を有する粒状層は、前記繊維層の前記一面の繊維に付着して形成されており、
且つ、前記粒状物を含んだ泡状組成物を前記繊維層の前記一面に塗布して得られた泡状塗工層から泡を破泡させて得られていることを要旨とする。
請求項に記載の湿式摩擦材用基材は、請求項1に記載の湿式摩擦材用基材において、前記粒状物として摩擦調整材を含むことを要旨とする。
請求項に記載の湿式摩擦材用基材は、請求項1又は2に記載の湿式摩擦材用基材において、前記繊維層の厚さが0.2mm以上1.3mm以下であることを要旨とする。
請求項4に記載の湿式摩擦材の製造方法は、抄造された繊維層の一面に、粒状物を含んだ泡状組成物を塗布して、前記粒状物を含んだ泡状塗工層を形成する泡状塗工層形成工程と、
前記泡状塗工層を構成する泡を破泡して気孔を有する粒状層を形成する破泡工程と、を備えることを要旨とする。
The present invention is as follows.
The wet friction material substrate according to claim 1, comprising: a fiber layer formed by paper forming; and a particulate layer having pores formed by particulate matter on one surface of the fiber layer,
The particulate layer having pores is formed by adhering to the fibers of the one surface of the fiber layer ,
And, wherein the granulate foam is foam breaking the from foam coating layer foam composition obtained was coated on the one surface of the fibrous layer including the gist that you have obtained.
The base material for a wet friction material according to a second aspect is the base material for a wet friction material according to the first aspect, wherein a friction modifier is included as the particulate matter.
The wet friction material substrate according to claim 3 is the substrate for a wet friction material according to claim 1 or 2, wherein the thickness of the fiber layer is 0.2 mm or more and 1.3 mm or less. I assume.
In the method for producing a wet friction material according to claim 4, a foamy composition containing particulates is applied to one surface of a formed fiber layer to form a foamy coated layer containing the particulates. Forming a foamy coating layer;
And forming a granular layer having pores by breaking the foam constituting the foam-like coating layer.

本湿式摩擦材用基材によれば、抄造によって形成された繊維層と、前記繊維層の一面に粒状物によって形成された気孔を有する粒状層と、を備え、この気孔を有する粒状層は、前記繊維層の一面の繊維に付着して形成されている。即ち、粒状物が気孔を有する粒状層として繊維層の一面にのみ偏在して形成されていることから、粒状物が繊維層の内部に存在せずに極めて顕著な偏在状態となっている。また、粒状層が繊維層の一面の繊維に付着していることから粒状層と繊維層が剥脱することもない。従って、従来に比べて更に顕著に摩擦調整材等の粒状物を偏在させることができるため、摩擦特性のように摩擦面に表出することでその特性を発揮する摩擦調整材等の粒状物を湿式摩擦材用基材の必要な面、すなわち摩擦面に高濃度に凝縮して存在させた湿式摩擦材用基材を得ることができる。これにより、従来に比べてより優れた摩擦特性を得ることができ、サイズ縮小や構成枚数の低減に対応できる湿式摩擦材を提供できる。また、摩擦調整材等の粒状物は摩擦面に表出することで粒状物が有する特性が発現するため、本発明の湿式摩擦材用基材では、配合する粒状物の全量を繊維層の一面に気孔を有する粒状層として配置でき、この粒状層の表面が湿式摩擦材用基材の摩擦面となるため、粒状物の特性が発現しない繊維層内部への配置が無くなり、原料として配合した粒状物の無駄を防止できる。更に、気孔を有する粒状層が繊維層の気孔を閉塞していないため、湿式摩擦材用基材として所望の気孔を維持して潤滑油に対し所望の吸油性を発揮できる。   According to the wet friction material substrate, the granular layer having the fibrous layer formed by paper-making and the granular layer having pores formed by the granular material on one surface of the fibrous layer is It adheres to the fiber of one side of the said fiber layer, and is formed. That is, since the particulate matter is formed unevenly on only one surface of the fiber layer as a particulate layer having pores, the particulate matter is not present inside the fibrous layer, and is in a very prominent localized state. Further, since the particulate layer adheres to the fibers on one side of the fibrous layer, the particulate layer and the fibrous layer are not exfoliated. Therefore, since particulate matter such as a friction modifier can be unevenly distributed more remarkably than in the conventional case, particulate matter such as a friction modifier exhibiting its characteristics by being exposed on a friction surface like friction characteristics It is possible to obtain a wet friction material substrate which is condensed to a necessary surface of the wet friction material substrate, that is, the friction surface. As a result, it is possible to obtain a friction characteristic superior to that in the prior art, and to provide a wet friction material capable of coping with size reduction and reduction in the number of components. In addition, since the particulate matter such as the friction modifier is exposed to the friction surface to develop the characteristics of the particulate matter, the substrate for the wet friction material of the present invention is one side of the fiber layer of the particulate matter to be blended. Can be arranged as a granular layer having pores, and the surface of this granular layer becomes the friction surface of the wet friction material substrate, so that the arrangement inside the fiber layer where the characteristics of the granular material do not appear disappears, the granular compounded as a raw material It is possible to prevent waste of things. Furthermore, since the particulate layer having pores does not block the pores of the fiber layer, it is possible to maintain desired pores as a substrate for a wet friction material and exert desired oil absorption to the lubricating oil.

本湿式摩擦材用基材の製造方法によれば、抄造された繊維層の一面に、粒状物を含んだ泡状組成物を塗布することで泡状塗工層を形成する泡状塗工層形成工程と、前記泡状塗工層から泡を破泡して気孔を有する粒状層を形成する破泡工程と、を備える。
この方法では泡状塗工層が泡状であるため、泡状塗工層内の粒状物が繊維層内部へ侵入せずに繊維層の一面に留めることができる。そのため繊維層の一面側のみに粒状層を配置できる。従って、湿式摩擦材用基材の表面に表出することで特性を発現する粒状物は、その特性を発現しない繊維層内部への粒状物の配置は無くなり、原料として配合した粒状物の無駄を防止できる。そして、粒状層は塗工層を構成する泡を破泡させることで得られるため気孔を有することなる。即ち、摩擦調整材等の粒状物を繊維層の一面側のみ偏在させても、粒状層には所望の気孔を有し、さらに、この気孔を有する粒状層は繊維層の一面に泡状で塗布された後に破泡させられて形成されるため粒状物が繊維層内部へ侵入せずに繊維層を閉塞しない。従って本発明の製造方法によって得られた湿式摩擦材用基材は基材全体に所望の気孔を有し、潤滑油に対し所望の吸油性を維持できる。
According to the method for producing a wet friction material substrate, a foamy coating layer is formed by applying a foamy composition containing particulate matter to one surface of a formed fiber layer to form a foamy coating layer. And forming a granular layer having pores by defoaming bubbles from the foam-like coating layer.
In this method, since the foam-like coating layer is foamy, the particulate matter in the foam-like coating layer can be retained on one side of the fiber layer without entering the inside of the fiber layer. Therefore, the particulate layer can be disposed only on one side of the fiber layer. Therefore, as for the granular material that expresses the characteristics by being exposed on the surface of the wet friction material substrate, the arrangement of the granular material inside the fiber layer which does not express the characteristics disappears, and waste of the granular material blended as a raw material It can prevent. And since a granular layer is obtained by breaking foam which constitutes a coating layer, it has pores. That is, even if particles such as friction modifiers are distributed only on one side of the fiber layer, the particle layer has desired pores, and the particle layer having pores is applied in a foam form to one surface of the fiber layer. Since the bubbles are formed after being bubbled, the particulate matter does not intrude into the inside of the fiber layer and does not clog the fiber layer. Accordingly, the wet friction material substrate obtained by the production method of the present invention has desired pores throughout the substrate, and can maintain desired oil absorption to the lubricating oil.

本発明の湿式摩擦基材の断面を模式的に示す説明図である。It is explanatory drawing which shows typically the cross section of the wet friction base material of this invention. 実施例1の湿式摩擦基材の表面を拡大(300倍)して示す説明図である。It is an explanatory view shown expanding the surface of the wet friction backing material of Example 1 (300 times). 実施例3の湿式摩擦基材の表面を拡大(300倍)して示す説明図である。It is explanatory drawing which expands and shows the surface of the wet friction base material of Example 3 (300 times). 比較例1の湿式摩擦基材の表面を拡大(300倍)して示す説明図である。It is explanatory drawing which expands and shows the surface of the wet friction base material of the comparative example 1 (300 times).

以下、本発明を、図を参照しながら説明する。ここで示す事項は例示的なもの及び本発明の実施形態を例示的に説明するためのものであり、本発明の原理と概念的な特徴とを最も有効に且つ難なく理解できる説明であると思われるものを提供する目的で述べたものである。この点で、本発明の根本的な理解のために必要で、ある程度以上に本発明の構造的な詳細を示すことを意図してはおらず、図面と合わせた説明によって本発明の幾つかの形態が実際にどのように具現化されるかを当業者に明らかにするものである。   Hereinafter, the present invention will be described with reference to the drawings. The matter set forth herein is for the purpose of illustration and description of the embodiments of the invention and is believed to be the most effective and easily understood explanation of the principles and conceptual features of the invention. For the purpose of providing what In this respect, it is not necessary to show the structural details of the present invention that is necessary for a fundamental understanding of the present invention, but to a certain extent or more, and some forms of the present invention will be described according to the description in conjunction with the drawings. It will be clear to the person skilled in the art how is actually embodied.

[1]湿式摩擦材用基材
本発明の湿式摩擦材用基材1は、抄造によって形成された繊維層11と、繊維層11の摩擦面側となる一面に、粒状物によって形成された気孔を有する粒状層12と、を備える。このうち、気孔を有する粒状層12は、繊維層11の一面の繊維に付着して繊維層11の一面上に、繊維層11の気孔111を閉塞しない態様で所望の気孔状態で形成されている(図1参照)。
[1] Base Material for Wet Friction Material The base material 1 for wet friction material of the present invention is a pore formed of particulate matter on one surface on the friction surface side of the fiber layer 11 formed by paper forming and the fiber layer 11 And a granular layer 12 having Among them, the particulate layer 12 having pores is attached to the fibers on one side of the fiber layer 11 and formed on one side of the fiber layer 11 in a desired pore state in a mode not blocking the pores 111 of the fiber layer 11 (See Figure 1).

繊維層11は、繊維を抄造することで繊維112が複雑に絡み合って形成された層である。繊維112の形態は特に限定されないが、例えば、長さが0.2〜1.3mm、径が0.1〜10μmが用いられる。
繊維112としては、有機繊維及び/又は無機繊維を利用できる。
このうち、有機繊維としては、ポリアミド系繊維、ポリエステル系繊維、アクリル系樹脂繊維及びアクリル繊維等の合成繊維、レーヨン等の再生繊維、セルロース繊維(パルプ)等の有機天然繊維などが挙げられる。これらは1種のみを用いてもよく2種以上を併用してもよい。このうち、ポリアミド系繊維としては、芳香族ナイロン繊維及び脂肪族ナイロン繊維が挙げられ、更には、芳香族ナイロン繊維(特に、全芳香族ナイロンを用いた繊維)としては、アラミド繊維が挙げられる。このアラミド繊維は、パラ系アラミド及びメタ系アラミドのいずれか一方又は両方を含むことができる。
一方、無機繊維としては、炭素系繊維(カーボン繊維、炭化繊維等含む)、単結晶繊維(ウォラストナイトフィラー等)、多結晶繊維(アルミナ繊維等)、非晶質繊維(ロックウール、ガラス繊維等)、金属繊維等が挙げられる。これらは1種のみを用いてもよく2種以上を併用してもよい。尚、各繊維の配合等は、必要に応じてなされる。
The fiber layer 11 is a layer formed by intertwining the fibers 112 in a complicated manner by forming the fibers. Although the form of the fiber 112 is not particularly limited, for example, a length of 0.2 to 1.3 mm and a diameter of 0.1 to 10 μm are used.
Organic fibers and / or inorganic fibers can be used as the fibers 112.
Among them, as organic fibers, synthetic fibers such as polyamide fibers, polyester fibers, acrylic resin fibers and acrylic fibers, regenerated fibers such as rayon, organic natural fibers such as cellulose fibers (pulp) and the like can be mentioned. These may use only 1 type and may use 2 or more types together. Among them, polyamide-based fibers include aromatic nylon fibers and aliphatic nylon fibers, and further, aromatic nylon fibers (in particular, fibers using wholly aromatic nylon) include aramid fibers. The aramid fiber can contain either or both of para-aramid and meta-aramid.
On the other hand, as inorganic fibers, carbon-based fibers (including carbon fibers, carbonized fibers, etc.), single crystal fibers (wollastonite filler, etc.), polycrystalline fibers (alumina fibers, etc.), amorphous fibers (rock wool, glass fibers) Etc.), metal fibers and the like. These may use only 1 type and may use 2 or more types together. The blending of each fiber is made as needed.

繊維層11の厚さは特に限定されないが、例えば、0.2mm以上1.3mm以下とすることができ、0.3mm以上1.0μm以下がより好ましい。
また、繊維層11は、湿式摩擦材の要求仕様に応じた所望の気孔111を有する。この気孔111は、抄造によって形成された繊維層11の繊維間の隙間である。この隙間が気孔111として存在することによって、湿式摩擦材用基材は潤滑油を吸収する吸油性が得られる。このように、繊維層11の気孔111の存在割合つまり気孔率は、吸油性と密接に関連していることから、10%以上80%以下とすることが好ましく、更には40%以上70%以下が好ましい。尚、この気孔率は、繊維層となる原紙を油に浸漬し、浸漬前後の質量及び体積からアルキメデス法を用いて算出される。即ち、原紙の浸漬前質量をW(g)、原紙の浸漬後質量をW(g)、原紙の体積をV(cm)、油の密度をρ(g/cm)とすると、繊維層の気孔率(%)=(W−W)×(1/ρ)×(1/V)×100である。
The thickness of the fiber layer 11 is not particularly limited, but can be, for example, 0.2 mm or more and 1.3 mm or less, and more preferably 0.3 mm or more and 1.0 μm or less.
Moreover, the fiber layer 11 has the desired pore 111 according to the required specification of a wet friction material. The pores 111 are gaps between the fibers of the fiber layer 11 formed by papermaking. The presence of the gaps as the pores 111 allows the wet friction material substrate to absorb oil so as to absorb lubricating oil. As described above, the existence ratio of the pores 111 of the fiber layer 11, that is, the porosity is closely related to the oil absorption, so it is preferably 10% to 80%, and more preferably 40% to 70%. Is preferred. The porosity is calculated by immersing the base paper to be a fiber layer in oil and using the Archimedes method from the mass and volume before and after immersion. That is, assuming that the pre-immersion mass of the base paper is W 0 (g), the post-immersion mass of the base paper is W 1 (g), the volume of the base paper is V 0 (cm 3 ), and the density of the oil is ρ (g / cm 3 ) The porosity of the fiber layer (%) = (W 1 −W 0 ) × (1 / ρ) × (1 / V 0 ) × 100.

粒状層12は、粒状物121によって形成された層である。この粒状層12は、繊維層11の摩擦面側の一面の繊維に付着して形成され、上述した繊維層11の気孔111を閉塞しない態様で形成されている。そして、繊維層11の気孔111を閉塞しない態様で繊維層11の摩擦面側の繊維の近傍に形成されていることがさらに好ましい。このように摩擦面側の繊維の近傍に摩擦面側の繊維に付着して粒状層12が形成されることで、粒状層12が有する気孔は、粒状層12が付着する繊維層11の一面が有する気孔と略同レベルの大きさを有する気孔となる。また、繊維層11の一面の気孔が十分大きいときには、粒状層12が有する気孔はこの繊維層11の一面の気孔よりも小さくした気孔とすることができる。そのため粒状層が繊維層の一面に付着して作製された湿式摩擦材用基材1の摩擦面での気孔、つまり粒状層の表面での気孔は、湿式摩擦材に要求される摩擦面において所望の気孔とすることができる。   The particulate layer 12 is a layer formed by the particulate matter 121. The granular layer 12 is formed by adhering to the fibers on one surface of the fiber layer 11 on the friction surface side, and is formed so as not to close the pores 111 of the fiber layer 11 described above. And it is still more preferable to form in the vicinity of the fiber of the friction surface side of the fiber layer 11 in the aspect which does not block the pore 111 of the fiber layer 11. Thus, the particulate layer 12 is formed by adhering to the fibers on the friction surface side in the vicinity of the fibers on the friction surface side, whereby the pores possessed by the granular layer 12 are one surface of the fiber layer 11 to which the particulate layer 12 adheres. The pores have a size substantially the same as that of the pores. Further, when the pores on one side of the fiber layer 11 are sufficiently large, the pores in the granular layer 12 can be made smaller than the pores on one side of the fiber layer 11. Therefore, the pores on the friction surface of the wet friction material substrate 1 prepared by adhering the granular layer to one surface of the fibrous layer, that is, the pores on the surface of the granular layer are desired in the friction surface required for the wet friction material The pores of the

このように、粒状層12が繊維層11の一面の繊維に付着しながら、この繊維の近傍に形成されている場合には、より所望の気孔状態が得られやすい。このような所望の気孔を有する粒状層12は、粒状物を含んだ泡状組成物を繊維層11の一面に塗布して得られた泡状塗工層から泡を破泡させることで得られる。即ち、本発明の湿式摩擦材用基材1の粒状層12は、粒状物121を泡状組成物に含ませて繊維層の摩擦面側の一面に塗工して得ることができる。このように粒状物121を含んだ組成物を泡状にして塗工することで粒状物が繊維層11の内部へ侵入することを抑制した状態で泡状組成物を塗工した泡状塗工層から泡を破泡させて粒状層12を形成している。従って繊維層11は粒状層12の粒状物121によってその内部が閉塞することがなく、粒状層12を形成する前の気孔状態を維持している。このように本発明の湿式摩擦材用基材1では、繊維層11に粒状層12を形成しても繊維層11の内部の気孔状態は粒状層を形成する前の状態と略同じ状態に維持され、粒状層も湿式摩擦材に要求される仕様によって泡状組成物の泡の状態を適宜選択することで粒状層12を形成する前の繊維層11の一面の状態と略同じ気孔状態や、より気孔を少なくした気孔状態など所望の気孔状態とすることが可能となる。   As described above, when the particulate layer 12 is formed in the vicinity of the fibers while adhering to the fibers on one side of the fiber layer 11, a more desirable pore state can be easily obtained. The particulate layer 12 having such desired pores can be obtained by breaking the foam from the foam-like coating layer obtained by applying the foam-like composition containing the particulate matter to one surface of the fiber layer 11 . That is, the granular layer 12 of the base material 1 for wet friction materials of the present invention can be obtained by including the granular material 121 in a foamy composition and coating it on one surface side of the fiber layer. Thus, the foam-like coating which applied the foamy composition in the state which suppressed that a granular material penetrates the inside of the fiber layer 11 by making the composition containing the granular material 121 into a foam and coating it. The foam is broken from the layer to form a particulate layer 12. Accordingly, the fiber layer 11 is not clogged by the particles 121 of the particle layer 12 and the pore state before the particle layer 12 is formed is maintained. As described above, in the wet friction material substrate 1 of the present invention, even if the granular layer 12 is formed in the fiber layer 11, the pore state inside the fibrous layer 11 is maintained substantially the same as the state before the granular layer is formed. The granular layer also has a substantially same pore state as that of one surface of the fiber layer 11 before forming the granular layer 12 by appropriately selecting the foam state of the foam-like composition according to the specifications required for the wet friction material, It is possible to obtain a desired pore state such as a pore state in which the pores are further reduced.

この粒状層12の気孔状態は、前述した繊維層11の気孔同様、潤滑油の吸収性能に影響を及ぼし、これが湿式摩擦材の摩擦特性等と関係している。特に形成された粒状層12の摩擦面となる面での表面占有率が重要であり、その値は1%以上60%以下とすることが好ましい。
この表面占有率は、湿式摩擦材用基材1の表面を覆う粒状層12の面積の割合を表わす。表面占有率は、17mm×23mmの大きさの粘着テープ{セロテープ(登録商標)}を、湿式摩擦材用基材1の表面(粒状層12が形成された表面)のうち、無作為に選択した5ヶ所に貼着した後、引き剥がし、得られた5枚の粘着テープの引剥し面の画像解析から、各粘着テープに占める非貼着箇所の合計面積S(cm)の平均値SAV(cm)を算出し、この平均値SAV(cm)が1枚の粘着テープの面積S(cm=17mm×23mm)に占める割合(%)として算出される。
The pore state of the granular layer 12, like the pores of the fiber layer 11 described above, affects the absorption performance of the lubricating oil, which is related to the friction characteristics and the like of the wet friction material. In particular, the surface occupancy on the surface to be the friction surface of the formed granular layer 12 is important, and the value is preferably 1% or more and 60% or less.
This surface occupancy represents the ratio of the area of the particulate layer 12 covering the surface of the wet friction material substrate 1. The surface occupancy ratio was randomly selected from the surface of the wet friction material substrate 1 (the surface on which the particulate layer 12 was formed), adhesive tape {Sellotape (registered trademark)} having a size of 17 mm × 23 mm. After pasting on 5 places, peeling off, from the image analysis of the peeled surface of the 5 adhesive tapes obtained, the average value S of the total area S 1 (cm 2 ) of the non-sticking area occupied in each adhesive tape AV (cm 2 ) is calculated, and this average value S AV (cm 2 ) is calculated as a percentage (%) of the area S 0 (cm 2 = 17 mm × 23 mm) of one adhesive tape.

粒状層12を構成する粒状物121は従来技術に使用されている各種材料が使用でき、特に限定されないが、湿式摩擦材用基材1の摩擦面で摩擦特性を発現する摩擦調整材等が挙げられる。粒状層を摩擦調整材等で形成することで湿式摩擦材用基材1は摩擦面にのみ摩擦調整材等を配置できることから摩擦特性等の特性を容易に制御することができる。そして、摩擦調整材等は単独でも、2種以上を併用することもできる。これによって摩擦特性等の特性を個別に、または複合させて湿式摩擦材用基材の摩擦面に容易に付与することが可能となる。
さらに、粒形状の粒状物121は、具体的には、平均粒径0.1μm以上1000μm以下が好ましく、2μm以上200μm以下が更に好ましい。尚、粒状物の平均粒径は、JIS Z8827−1の「静的画像解析法」に準拠した値とする。
The particulate material 121 constituting the particulate layer 12 may be any of various materials used in the prior art, and is not particularly limited, but a friction modifier or the like exhibiting friction characteristics on the friction surface of the wet friction material substrate 1 is mentioned. Be By forming the granular layer with a friction control material or the like, since the friction control material or the like can be disposed only on the friction surface of the wet friction material substrate 1, characteristics such as friction characteristics can be easily controlled. The friction modifiers may be used alone or in combination of two or more. This makes it possible to easily impart properties such as friction properties to the friction surface of the wet friction material substrate individually or in combination.
Furthermore, specifically, the average particle diameter is preferably 0.1 μm or more and 1000 μm or less, and more preferably 2 μm or more and 200 μm or less. In addition, let the average particle diameter of a granular material be a value based on the "static image-analysis method" of JISZ8827-1.

粒状層12の厚さは特に限定されないが、例えば、0.1μm以上1000μm以下とすることができ、2μm以上400μm以下がより好ましい。即ち、粒状層12は、泡状組成物に配された接着剤によって粒状物121同士結着され、さらに粒状層12が繊維層11に接着剤によって付着しているが、湿式摩擦材として使用されるときに剪断力が粒状層に加わるため、厚みが厚いと破壊や剥離が起き易くなるためである。   The thickness of the granular layer 12 is not particularly limited, but may be, for example, 0.1 μm or more and 1000 μm or less, and more preferably 2 μm or more and 400 μm or less. That is, although the granular layer 12 is bound to each other by the adhesive disposed in the foamy composition and the granular layer 12 is further adhered to the fiber layer 11 by the adhesive, it is used as a wet friction material At the same time, shear force is applied to the granular layer, so if the thickness is thick, breakage and peeling are likely to occur.

このように、本発明の湿式摩擦基材1では、粒状層12の粒状物121が繊維層11内に存在させることなく、粒状物121を繊維層11の一面側に留め置くことができる。従って、従来に比べて更に顕著に粒状物121を、繊維層11の一面側のみに偏在させた湿式摩擦基材を得ることができる。
このような形態で、粒状物121として摩擦調整材を選択した場合には、配合した摩擦調整材の実質全量を繊維層11の一面側のみに偏在させることができるため少量で摩擦調整機能を発現させることができる。即ち、湿式摩擦基材1の内部に、使用時の摩擦に関与しない不要な摩擦調整材を含有させることなく、使用時に最も必要な箇所つまり摩擦面に摩擦調整材を集中的に配置することで極めて効率良く摩擦調整ができる。
Thus, in the wet friction substrate 1 of the present invention, the particulate matter 121 can be held on one side of the fiber layer 11 without the particulate matter 121 of the particulate layer 12 being present in the fiber layer 11. Therefore, it is possible to obtain a wet friction substrate in which the particulate matter 121 is unevenly distributed only on one surface side of the fiber layer 11 more remarkably than in the prior art.
In such a form, when a friction modifier is selected as the particulate matter 121, a substantial amount of the blended friction modifier can be unevenly distributed only on one surface side of the fiber layer 11, and a small amount of friction modifier is expressed. It can be done. That is, the friction control material is intensively disposed at the most necessary place in use, ie, the friction surface, without containing an unnecessary friction control material not involved in the friction in use inside the wet friction substrate 1. Friction can be adjusted very efficiently.

このように、本発明の湿式摩擦材用基材1では、摩擦調整材を粒状物121として使用したときには、摩擦調整材自体を抄造時の分散液に配合することがなく、事後的に摩擦調整材を所望の特性を得るのに必要な量だけを塗工によって繊維層11上の摩擦面側に粒状層12として形成することとなる。   As described above, in the wet friction material substrate 1 according to the present invention, when the friction modifier is used as the particulate matter 121, the friction modifier itself is not blended in the dispersion during paper making, and the friction adjustment is performed afterward. By coating only the amount necessary to obtain the desired properties of the material, the granular layer 12 is formed on the friction surface side on the fiber layer 11.

尚、本発明の湿式摩擦材用基材1には、その粒状層12が、粒状物121を含んだ泡状組成物を繊維層11の一面に塗布して得られた泡状塗工層から泡を破泡させて得られたものが含まれる。この粒状層12は、得られた状態において、既に泡は消失されている為、製造過程で泡が介在されたことを、粒状層12を有した湿式摩擦材用基材1の構造又は特性を解析することによって、当該湿式摩擦材用基材についての構造又は特性を明記して直接特定することは技術的に不可能である。また、仮に何らの方法によって当該構造又は特性を解析でき得るとしても、特許出願の性質上、迅速性等を必要とすることに鑑みて、特定する作業を行うことには著しく過大な経済的支出や時間を要することになる。即ち、当該湿式摩擦材用基材をその構造又は特性を明記して直接特定することには、不可能・非実際的事情が存在する。   In the wet friction material substrate 1 of the present invention, the granular layer 12 is formed by applying a foamy composition containing the particulate matter 121 to one surface of the fiber layer 11 from a foamy coating layer Included are those obtained by breaking the foam. In this granular layer 12, the foam has already disappeared in the obtained state, and therefore, it is known that the foam was interposed in the manufacturing process, the structure or characteristics of the wet friction material substrate 1 having the granular layer 12. It is technically impossible to specify and directly specify the structure or characteristics of the wet friction material substrate by analysis. In addition, even if it is possible to analyze the structure or characteristics by any method, the cost of the operation to be identified is extremely excessive for performing the identification work in view of the need for promptness etc. in the nature of the patent application. It will take some time. That is, there are impossible and unpractical situations in directly specifying the structure or characteristics of the wet friction material substrate.

[2]湿式摩擦材用基材の製造方法
本発明の湿式摩擦材用基材1の製造方法は、泡状塗工層形成工程と破泡工程とを備える。これらの泡状塗工層形成工程及び破泡工程は、同時に進行させてもよく、泡状塗工層形成工程を終えた後に破泡工程を行ってもよい。
[2] Method of Manufacturing Base Material for Wet Friction Material The method of manufacturing the base material 1 for wet friction material of the present invention comprises a foam-like coating layer forming step and a bubble-breaking step. The step of forming a foamy coating layer and the step of defoaming may be performed simultaneously, or the step of defoaming may be performed after completing the step of forming a foamy coating layer.

このうち、泡状塗工層形成工程は、抄造された繊維層11の表面に、粒状物121を含んだ泡状組成物を塗布して泡状塗工層を形成する工程である。   Among these, the foam-like coating layer forming step is a step of applying a foam-like composition containing the particulate matter 121 to the surface of the formed fiber layer 11 to form a foam-like coating layer.

泡状組成物は、粒状物121を含む組成物を泡立てて得られたものをいう。組成物には少なくとも粒状物、気泡剤、接着剤を配合した主材料を液状媒体(水、有機溶媒等)に分散させたものであり、必要に応じてこの主材料に増粘剤、分散剤等の添加剤を加えた配合材料を液体溶媒に分散させたものである。泡状組成物は、この組成物を気泡剤によって泡立たせたものである。
このうち、気泡剤は、気泡の形成を促す成分であり、具体的には、各種の界面活性剤を利用することができる。接着剤は、繊維層の繊維と粒状物を付着し、粒状物同士を結合させる成分である。具体的には、ポリビニルエーテル、ポリビニルアルコール、ポリ酢酸ビニル、水溶性アクリルポリマー等の水溶性ポリマーを利用できる。
The foamy composition refers to one obtained by frothing the composition containing the particulate matter 121. In the composition, a main material containing at least particulates, a foaming agent, and an adhesive is dispersed in a liquid medium (water, organic solvent, etc.), and if necessary, the main material is a thickener, a dispersing agent Etc. are dispersed in a liquid solvent. The foamy composition is obtained by foaming the composition with a foaming agent.
Among these, the foaming agent is a component that promotes the formation of bubbles, and specifically, various surfactants can be used. The adhesive is a component that adheres the fibers and particles of the fiber layer and bonds the particles. Specifically, water-soluble polymers such as polyvinyl ether, polyvinyl alcohol, polyvinyl acetate, and water-soluble acrylic polymers can be used.

粒状物は、得たい特性を繊維層上に発現させるものが選択され、従来技術に使用されている各種材料が使用できる。
粒状物、気泡剤の配合は特に限定されないが、粒状物に摩擦調整材を選択したときには例えば、粒状物を5質量%以上40質量%以下、気泡剤を5質量%以上20質量%以下、の割合とすることができる。この範囲内にすることで粒状層が効果的に摩擦調整機能を発揮し、さらに繊維層上からの剥離や粒状層の破壊が起き難く湿式摩擦材の長期使用が可能となる。
これらの成分の配合順序等は限定されず、例えば、必要な材料を一括配合した液体を泡立ててもよく、泡立てながら各種成分を添加してもよい。
The particulates are selected to give the desired properties on the fiber layer, and various materials used in the prior art can be used.
There are no particular limitations on the composition of the particulate matter and the foaming agent, but when the friction modifier is selected for the particulate matter, for example, 5% by mass or more and 40% by mass or less of the particulate matter and 5% by mass or more and 20% by mass or less of the foaming agent It can be a percentage. By being in this range, the particulate layer effectively exerts a friction adjusting function, and further, peeling from the fiber layer and breakage of the particulate layer hardly occur, and the long-term use of the wet friction material becomes possible.
The order of blending these components is not limited, and for example, a liquid in which necessary materials are batch-blended may be bubbled or various components may be added while foaming.

更に、泡状組成物を調製する際には、必要に応じて泡状組成物の泡の平均径と粒状物の平均粒径の比を制御することが好ましい。泡の平均径に対する粒状物の平均粒径の比は、0.005以上0.5以下が好ましく、0.01から0.5以下がより好ましい。泡状組成物の泡の平均径と粒状物の平均粒径の比が0.005未満の場合には、粒状物の平均粒径以下になる。泡状組成物の泡の平均粒径と粒状物の平均粒径の比が0.5を超える場合には、泡が形成しにくくなる。ここで、粒状物の平均粒径は、前述の通り、0.1μm以上1000μm以下が好ましく、2μm以上200μm以下が更に好ましい。一方、泡の平均径は、20μm以上500μm以下が好ましく、30μm以上300μm以下が更に好ましい。泡の平均径は、光学顕微鏡を介した記録した記録画像を用い、記録画像内で無作為に選択した50個の泡径を実測(記録画像上で実測)して得た各泡径の平均値である。   Furthermore, when preparing the foamy composition, it is preferable to control the ratio of the average diameter of the foam of the foamy composition to the average particle size of the granules, as necessary. 0.005 or more and 0.5 or less are preferable, and, as for the ratio of the average particle diameter of the granular material to the average diameter of a bubble, 0.01 to 0.5 or less are more preferable. When the ratio of the average diameter of the foam of the foamy composition to the average particle diameter of the particles is less than 0.005, the average particle diameter of the particles is equal to or less than that of the particles. When the ratio of the average particle size of the foam of the foamy composition to the average particle size of the particulate matter exceeds 0.5, the foam is less likely to be formed. Here, as described above, the average particle diameter of the particulate matter is preferably 0.1 μm to 1000 μm, and more preferably 2 μm to 200 μm. On the other hand, 20 micrometers or more and 500 micrometers or less are preferable, and, as for the average diameter of a bubble, 30 micrometers or more and 300 micrometers or less are still more preferable. The average diameter of the bubbles was obtained by measuring the diameters of 50 randomly selected bubbles in the recorded image (measured on the recorded image) using the recorded image recorded through an optical microscope. It is a value.

このような泡状組成物は、泡状塗工層形成工程によって繊維層12の一面に塗布される。そして、その塗布は、各種塗工方法を適宜選択して行われる。具体的には、塗工用ローラに泡状組成物を付けて、このローラを繊維層12に押し付けることによって塗工することができる。また、コーターを用いてコーティングによって塗工することができる。
また、繊維層11への泡状組成物の塗布量は1質量以上10質量%以下と少量で充分あり、このような少量の塗布量で良好な摩擦特性を得た湿式摩擦材用基材となる。そして、泡状塗工層形成工程は、抄造した繊維層11を乾燥させる前の湿潤段階や乾燥後の乾燥段階で実施することができる。
このように泡状組成物を繊維層11に塗布する泡状塗工層形成工程では、形成する塗工層が泡状であるため、繊維層11内部へ泡状組成物が浸透せず、泡状塗工層として繊維層11の表面の繊維に付着して繊維層11の表面に留めることができる。また、泡状塗工層は、これを構成する複数の泡同士の境界部分に粒状物121を包含した状態となっている。そして泡状組成物中には接着剤が含有されているためこの接着剤が粒状物表面に付着している。この状態で泡を破泡すると、粒状物121同士が付着している接着剤によって結合し粒状層12が形成される。このとき、結合した粒状物は全てが結合する訳ではなく泡の存在によって部分的に結合がなされない部分が生ずる。この結合が阻害された部分が気孔となることから、粒状層12は気孔を有することとなる。そして、粒状層12は繊維層11に浸透せずに形成されていることから繊維層11の気孔111が粒状物121によって閉塞されず、気孔111を維持することができる。このように、粒状層12の気孔形成と繊維層11の気孔維持によって湿式摩擦材用基材1の潤滑油に対する吸油性が維持されるのである。
Such a foamy composition is applied to one surface of the fiber layer 12 by the foamy coating layer forming step. And the application is performed by appropriately selecting various coating methods. Specifically, the composition can be coated by applying a foamy composition to a coating roller and pressing the roller against the fiber layer 12. Moreover, it can coat by coating using a coater.
Further, the amount of the foam-like composition applied to the fiber layer 11 is sufficient at a small amount of 1 to 10% by mass, and a substrate for a wet friction material having good friction characteristics with such a small amount of application Become. And a foamy coating layer formation process can be implemented in the wet stage before making the paper layer 11 dried, and the drying stage after drying.
Thus, in the foam-like coating layer forming step of applying the foam-like composition to the fiber layer 11, the foam-like composition does not permeate into the inside of the fiber layer 11 because the coating layer to be formed is foamy. Can be attached to the fibers of the surface of the fiber layer 11 as a cross-shaped coating layer and can be retained on the surface of the fiber layer 11. Moreover, the foam-like coating layer is in a state in which the particulate matter 121 is included in the boundary portion between the plurality of bubbles constituting the foam-like coating layer. And since the foam-like composition contains an adhesive, the adhesive adheres to the surface of the particulate matter. When the foam is broken in this state, the particulates 121 are bonded together by the adhering adhesive to form the particulate layer 12. At this time, the bound particles are not all bound, but the presence of the foam results in partially unbonded portions. The granular layer 12 has pores because the part where the binding is inhibited becomes pores. And since the granular layer 12 is formed without penetrating into the fiber layer 11, the pores 111 of the fibrous layer 11 are not blocked by the granular material 121, and the pores 111 can be maintained. Thus, the oil absorption of the wet friction material substrate 1 with respect to the lubricating oil is maintained by the pore formation of the granular layer 12 and the pore maintenance of the fiber layer 11.

破泡工程は、泡状塗工層を構成する泡を破泡して粒状層12を形成する工程である。
破泡工程において破泡は、どのように行ってもよい。具体的には、放置することによって自然に破泡させることができる。また、加熱によって破泡することができる。更には、加圧よって破泡することができる。また、押圧よって破泡することができる。これらの破泡方法は、1種のみを用いてもよく2種以上を併用してもよい。
The foam breaking step is a step of breaking the foam constituting the foam-like coating layer to form the particulate layer 12.
In the bubbling step, bubbling may be performed in any manner. Specifically, the foam can be naturally broken by leaving it to stand. In addition, it can be broken by heating. Furthermore, bubbles can be broken by pressure. Also, the foam can be broken by pressing. These foam-breaking methods may be used alone or in combination of two or more.

破泡工程によって形成された粒状層12は、その表面(粒状層12における繊維層11の一面に付着した面と反対の面)が湿式摩擦材用基材1の摩擦面となり、その摩擦面に占める粒状層の面積割合が、前述の表面占有率となる。この表面占有率は、前述の通り、1%以上60%以下の範囲が好ましい。この範囲とすることで、潤滑油の吸油性が充分維持されることで摩擦面での良好な摩擦特性を有する、良好な湿式摩擦材用基材1が得られる。   The surface (the surface opposite to the surface attached to one surface of the fiber layer 11 in the particle layer 12) of the particle layer 12 formed by the cell-breaking process is the friction surface of the wet friction material substrate 1, and the friction surface The area ratio of the granular layer to occupy becomes the above-mentioned surface occupancy. As described above, the surface occupancy is preferably in the range of 1% to 60%. Within this range, the oil absorption property of the lubricating oil is sufficiently maintained, whereby a good wet friction material substrate 1 having good friction characteristics on the friction surface can be obtained.

以下、本発明を実施例によって具体的に説明する。
[1]実施例品の調製
実施例1−2の湿式摩擦材用基材を調製した。
(1)泡状組成物の調製
アルキルエーテル系の気泡剤10質量%、ポリビニルエーテル系の接着剤10質量%、有機系の摩擦調整材(粒状物)20質量%、液状溶媒の水60質量%を混合して、全量100質量%の液体を得た。この得られた液体を攪拌混合することでアルキルエーテル系の気泡剤の作用により混合溶液は泡立ち泡状組成物とした。
気泡剤の配合量は、5質量%以上30質量%以下の範囲が好ましい。気泡剤の配合量は、5質量%未満の場合には、気泡が不足し、30質量%を超える場合には、塗工性が低下する。
接着剤の配合量は、5質量%以上30質量%以下の範囲が好ましい。接着剤の配合量は、5質量%未満の場合には、基材との接着性が得られない懸念があり、30質量%を超える場合には、塗工性が低下する。
粒状物の配合量は、5質量%以上40質量%以下の範囲が好ましい。粒状物の配合量は、5質量%未満の場合には、所望の摩擦特性が得られない懸念があり、40質量%を超える場合には、塗工性が低下する。
(2)泡状塗工層形成工程
上記(1)で得られた泡状組成物を塗工用ローラに付けて抄造により形成された繊維層11の一面に、実施例1では塗布量が繊維層11に対し0.04質量%となるように、実施例2では0.16質量%と実施例1の4倍多く塗布して繊維層11に泡状塗工層を形成した。本実施例では繊維層11は予め乾燥させた状態のものを使用した。
尚、上述の塗布量(実施例1:0.04質量%、実施例2:0.16質量%、実施例3:0.16質量%)は、粒状層と繊維層との合計に対する粒状層の質量割合(粒状層/(粒状層+繊維層))を意味する。
(3)破泡工程
上記(2)で得られた泡状塗工層そのまま放置させて、泡が自然に破泡されるのを待ち、粒状層12を形成した。
(4)表面状態の確認
上記工程によって形成させた実施例1の粒状層11の表面を、光学顕微鏡により300倍に拡大したデジタル画像を記録し、図2にその一部を示した。ここで、画像解析により繊維層11に付着した粒状層12の湿式摩擦材用基材1の摩擦面における粒状物121による表面占有率は8%であった。
Hereinafter, the present invention will be specifically described by way of examples.
[1] Preparation of Example Article A wet friction material substrate of Example 1-2 was prepared.
(1) Preparation of foamy composition 10% by mass of an alkyl ether-based foaming agent, 10% by mass of a polyvinyl ether-based adhesive, 20% by mass of an organic friction modifier (particulate matter), 60% by mass of water of a liquid solvent Were mixed to obtain a liquid of 100% by mass in total. By stirring and mixing the obtained liquid, the mixed solution becomes a foamy composition by the action of the alkyl ether-based foaming agent.
The blending amount of the foaming agent is preferably in the range of 5% by mass to 30% by mass. When the amount of the foaming agent is less than 5% by mass, the amount of bubbles is insufficient, and when it exceeds 30% by mass, the coating property is reduced.
The blending amount of the adhesive is preferably in the range of 5% by mass to 30% by mass. If the blending amount of the adhesive is less than 5% by mass, there is a concern that adhesion with the substrate can not be obtained, and if it exceeds 30% by mass, the coatability is reduced.
The blending amount of the particulate matter is preferably in the range of 5% by mass to 40% by mass. If the amount of the granular material is less than 5% by mass, there is a concern that the desired friction characteristics can not be obtained, and if it exceeds 40% by mass, the coatability is reduced.
(2) Foam-Like Coating Layer Forming Step In Example 1, the coating amount of fibers is applied to one surface of the fiber layer 11 formed by applying the foam-like composition obtained in the above (1) to a roller for coating The foam-like coating layer was formed on the fiber layer 11 by applying 0.16% by mass in Example 2 and 4 times that in Example 1 so as to be 0.04% by mass with respect to the layer 11. In the present embodiment, the fiber layer 11 is used in a state of being dried in advance.
In addition, the above-mentioned application quantity (Example 1: 0.04 mass%, Example 2: 0.16 mass%, Example 3: 0.16 mass%) is a granular layer to the sum total of a granular layer and a fiber layer. Mean the mass ratio of (particulate layer / (particulate layer + fiber layer)).
(3) Bubble-breaking step The foam-like coating layer obtained in the above (2) was allowed to stand as it was, and it was waited for the bubbles to break naturally, thereby forming the granular layer 12.
(4) Confirmation of Surface State A digital image in which the surface of the granular layer 11 of Example 1 formed by the above steps was enlarged 300 times with an optical microscope was recorded, and a part of it was shown in FIG. Here, according to image analysis, the surface occupancy by the particulate matter 121 on the friction surface of the wet friction material substrate 1 of the particulate layer 12 attached to the fiber layer 11 was 8%.

実施例3の湿式摩擦材用基材を調製した。
(1)非泡状組成物の調製
実施例1に使用した泡状組成物から気泡剤を除いた成分、つまりポリビニルエーテル系の接着剤10質量%、有機系の摩擦調整材20質量%、液状溶媒の水70質量%を混合して、粒状層を形成する塗工用の分散剤(非泡状組成物)を得た。
(2)粒状層形成工程
上記(1)で得られた非泡状組成物を実施例品と同様に塗布量0.16質量%で塗工用ローラを用いて繊維層の一面に塗工し粒状層を形成した。
(3)表面状態の確認
上記(2)で得られた粒状層の表面を、光学顕微鏡により300倍に拡大したデジタル画像を記録し、図3にその一部を示した。
A wet friction material substrate of Example 3 was prepared.
(1) Preparation of non-foaming composition Component obtained by removing the foaming agent from the foamy composition used in Example 1, that is, 10% by mass of polyvinyl ether adhesive, 20% by mass of organic friction modifier, liquid 70% by mass of water as a solvent was mixed to obtain a coating dispersant (non-foamy composition) for forming a particulate layer.
(2) Granular layer formation process The non-foamy composition obtained in the above (1) is coated on one surface of the fiber layer using a coating roller at a coating amount of 0.16% by mass as in the example product. A granular layer was formed.
(3) Confirmation of Surface State A digital image in which the surface of the granular layer obtained in the above (2) was magnified 300 times with an optical microscope was recorded, and a part thereof is shown in FIG.

[2]比較例品の調製
比較例1の湿式摩擦材用基材を調製した。
〈1〉比較例1
(1)湿式摩擦材用基材の調整
繊維を抄造する際の分散液に実施例と同じ有機系の摩擦調整材を20質量%配合させて抄造し、従来と同じ湿式摩擦材用基材を得た。
(2)表面状態の確認
実施例1と同様、湿式摩擦材用基材の表面を光学顕微鏡により300倍に拡大したデジタル画像を記録し、図4にその一部を示した。
[2] Preparation of Comparative Example A wet friction material base of Comparative Example 1 was prepared.
<1> Comparative Example 1
(1) Preparation of base material for wet friction material: 20% by mass of the same organic type friction modifier as in the example is compounded in the dispersion for forming the fiber and paper-formed, and the same base material for wet friction material as in the prior art Obtained.
(2) Confirmation of Surface Condition As in Example 1, a digital image in which the surface of the wet friction material substrate was enlarged 300 times with an optical microscope was recorded, and a part of it was shown in FIG.

[3]湿式摩擦材用基材の評価
〈1〉静摩擦係数μsの測定
上記[1]で得られた実施例1−2及び上記[2]で得られた比較例1の各湿式摩擦材用基材にフェノール樹脂を含浸させた後、含浸させた湿式摩擦材用基材を金属製の平板リング状のコアプレート(外径140mm、内径110mm)の表裏の両面に加圧加熱により接合して、評価用湿式摩擦材を得た。
上記評価用湿式摩擦材を各々3枚利用して、SAE摩擦試験機(SAE#2)を用い、回転数4000rpm、面圧0.7MPa、油温100℃、油量Is:0.343kg/m(完全浸漬)の条件でμsの測定を行った。その結果を表1に示した。
[3] Evaluation of base material for wet friction material <1> Measurement of static friction coefficient μs For each wet friction material of Example 1-2 obtained in the above [1] and Comparative example 1 obtained in the above [2] After impregnating the base material with a phenolic resin, the base material for wet friction material impregnated is joined by pressure heating to both the front and back of a flat ring-shaped core plate made of metal (outer diameter 140 mm, inner diameter 110 mm). , The wet friction material for evaluation was obtained.
Using 3 pieces of each of the above wet friction materials for evaluation, using an SAE friction tester (SAE # 2), rotation speed 4000rpm, contact pressure 0.7MPa, oil temperature 100 ° C, oil amount Is: 0.343kg / m The measurement of μs was performed under the condition of 3 (full immersion). The results are shown in Table 1.

μsの測定の結果から、本発明の実施例1〜3では摩擦調整材である粒状物の湿式摩擦材用基材における含有量を大幅に減少させても従来品である比較例1と略同等の静摩擦係数を発現可能であることが明らかになった。 From the result of the measurement of μs, in Examples 1 to 3 of the present invention, even if the content of the granular material as the friction modifier in the wet friction material substrate is significantly reduced, it is substantially the same as Comparative Example 1 which is the conventional product. It became clear that the coefficient of static friction of

〈2〉μ−Vの測定
上記[1]で得られた実施例2〜3及び上記[2]で得られた比較例1の各湿式摩擦材を、各々3枚利用して、LVFA試験機を用い、回転数0−1000−0rpm、面圧0.7MPa、油温40℃、油量1000mL/minの条件でμ−Vの測定を行った。その結果を表2に示した。
<2> Measurement of μ-V An LVFA test machine using three pieces of the wet friction material of each of Examples 2 to 3 obtained in the above [1] and the comparative example 1 obtained in the above [2]. The μ-V was measured under the conditions of a rotation speed of 0-1000-0 rpm, a surface pressure of 0.7 MPa, an oil temperature of 40 ° C., and an oil amount of 1000 mL / min. The results are shown in Table 2.

μ−Vの測定の結果から、実施例3は、表1に示すように、粒状物の含有量が大幅に少なくとも優れた静摩擦係数を発現できるものの、μ−Vの測定では、比較例1と同様の結果に留まることが分かる。これに対して実施例2は、表1に示すように、粒状物の含有量が大幅に少なくとも優れた静摩擦係数を発現できることに加えて、従来品である比較例1に比べて勾配が正勾配となりμ−V特性が改良されていることが分かる。 From the result of the measurement of μ-V, as shown in Table 1, in Example 3, although the content of the particulate matter can express at least the excellent coefficient of static friction significantly, in the measurement of μ-V, Comparative Example 1 and It can be seen that the same result remains. On the other hand, in Example 2, as shown in Table 1, in addition to the fact that the content of the particulate matter can at least significantly develop the excellent static friction coefficient, the gradient is a positive gradient compared to Comparative Example 1 which is the conventional product. It can be seen that the μ-V characteristic is improved.

(3)表面状態の比較
図2(実施例1)と図4(比較例1)を比較すると、実施例1は配合量を大幅に減少させても、従来の抄紙のように粒状物を繊維と共に抄造した湿式摩擦材用基材と略同じ量の粒状物を湿式摩擦材用基材の摩擦面に配することができることが明らかになった。
更に、図2(実施例1)と図3(実施例3)を比較すると、抄造した繊維層に粒状物を泡状にしないで塗工(非泡塗工)すると、繊維層11の繊維間に形成された気孔111を粒状物121が閉塞してしまう(実施例3)が、泡状にして塗工(泡塗工)すると繊維層11内部に粒状物が存在せず気孔111を閉塞しない(実施例1)ことが分かる。
以上実施例と比較例の表面観察と評価結果から、本発明は、従来の繊維層内へ摩擦調整材等の粒状物を無駄に含有させないで必要な量だけを粒状層として繊維層の摩擦面側となる一面に付着させて形成し、これによって摩擦特性等の所望特性を摩擦面に発現させることができる。この際、粒状層は繊維層の摩擦面側の気孔を閉塞することがなく所望の気孔を有し潤滑油に対し従来品同様の吸油性を維持可能としている。従って、本発明の湿式摩擦材用基材は、粒状物の配合量を大幅に減して湿式摩擦材用基材の摩擦面において所望特性を容易に得ることができ、性能向上、軽量化、コスト低減を可能とする。
(3) Comparison of Surface Conditions Comparing FIG. 2 (Example 1) and FIG. 4 (Comparative Example 1), even if Example 1 significantly reduces the compounding amount, it is possible to use fibers as in conventional paper making as in conventional papermaking. It has become clear that substantially the same amount of particles as the wet friction material base material produced can be disposed on the friction surface of the wet friction material base material.
Furthermore, when FIG. 2 (Example 1) and FIG. 3 (Example 3) are compared, when the granular material is applied to the formed fiber layer without foaming it (non-foamed coating), the fibers of the fiber layer 11 are The particulate matter 121 clogs the pores 111 formed in (Example 3), but when it is formed into a foam and applied (foam coating), the particulate matter does not exist inside the fiber layer 11 and the pores 111 are not clogged. It can be seen that (Example 1).
From the surface observation and evaluation results of the examples and comparative examples described above, according to the present invention, the friction surface of the fiber layer is treated as a granular layer without using waste particles such as friction modifiers in the conventional fiber layer. It is made to adhere to one side which becomes a side, and, thereby, desired characteristics, such as a frictional characteristic, can be expressed on a frictional surface. At this time, the granular layer does not close the pores on the friction surface side of the fiber layer, has desired pores, and can maintain the same oil absorption as that of the conventional product with respect to the lubricating oil. Therefore, the base material for wet friction materials of the present invention can easily obtain desired properties on the friction surface of the base material for wet friction materials by significantly reducing the compounding amount of the particulate matter, improving the performance, reducing the weight, Enables cost reduction.

尚、本発明においては、上記の具体的実施例に示すものに限られず、目的、用途に応じて本発明の範囲内で種々変更した実施例とすることができる。   In the present invention, the present invention is not limited to the specific examples described above, and various changes may be made within the scope of the present invention according to the purpose and application.

本発明の湿式摩擦基材及び湿式摩擦材の用途は特に限定されず、例えば、自動車(四輪自動車、二輪自動車等)、鉄道車両、船舶、飛行機等において広く適用される。このうち自動車用品としては、自動変速機(オートマチックトランスミッション、AT)に好適に用いられる。   The application of the wet friction base material and the wet friction material of the present invention is not particularly limited. Among these, as an automobile article, it is suitably used for an automatic transmission (automatic transmission, AT).

1;湿式摩擦基材、
11;繊維層、111;気孔、112;繊維、
12;粒状層、121;粒状物。
1; Wet friction substrate,
11; fiber layer, 111; pores, 112; fiber,
12; granular layer, 121; granular material.

Claims (4)

抄造によって形成された繊維層と、前記繊維層の一面に粒状物によって形成された気孔を有する粒状層と、を備え、
前記気孔を有する粒状層は、前記繊維層の前記一面の繊維に付着して形成されており、
且つ、前記粒状物を含んだ泡状組成物を前記繊維層の前記一面に塗布して得られた泡状塗工層から泡を破泡させて得られていることを特徴とする湿式摩擦材用基材。
And a particulate layer having pores formed by particulate matter on one surface of the fibrous layer.
The particulate layer having pores is formed by adhering to the fibers of the one surface of the fiber layer ,
And, a wet friction material characterized that you have obtained foam is foam breaking the said foam composition containing particulates from foam coating layer, wherein the obtained coated on one surface of the fibrous layer Base material.
前記粒状物として、摩擦調整材を含むことを特徴とする請求項1に記載の湿式摩擦材用基材。   The substrate for a wet friction material according to claim 1, wherein the granular material includes a friction modifier. 前記繊維層の厚さが、0.2mm以上1.3mm以下であることを特徴とする請求項1又は2に記載の湿式摩擦材。The thickness of the said fiber layer is 0.2 mm or more and 1.3 mm or less, The wet friction material of Claim 1 or 2 characterized by the above-mentioned. 抄造された繊維層の一面に、粒状物を含んだ泡状組成物を塗布して、前記粒状物を含んだ泡状塗工層を形成する泡状塗工層形成工程と、
前記泡状塗工層を構成する泡を破泡して気孔を有する粒状層を形成する破泡工程と、を備えることを特徴とする湿式摩擦材用基材の製造方法。
A foamy coating layer forming step of applying a foamy composition containing particulate matter to one surface of the formed fiber layer to form a foamy coating layer containing the particulate matter;
And b) a foam-breaking step of breaking the foam constituting the foam-like coating layer to form a particulate layer having pores.
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